Product NDC: | 68387-450 |
Proprietary Name: | Silver Sulfadiazine |
Non Proprietary Name: | Silver Sulfadiazine |
Active Ingredient(s): | 10 mg/g & nbsp; Silver Sulfadiazine |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68387-450 |
Labeler Name: | Keltman Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA018578 |
Marketing Category: | ANDA |
Start Marketing Date: | 20070310 |
Package NDC: | 68387-450-01 |
Package Description: | 50 g in 1 JAR (68387-450-01) |
NDC Code | 68387-450-01 |
Proprietary Name | Silver Sulfadiazine |
Package Description | 50 g in 1 JAR (68387-450-01) |
Product NDC | 68387-450 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Silver Sulfadiazine |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20070310 |
Marketing Category Name | ANDA |
Labeler Name | Keltman Pharmaceuticals Inc. |
Substance Name | SILVER SULFADIAZINE |
Strength Number | 10 |
Strength Unit | mg/g |
Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |